The objective of the study is a multi-center prospective registry to collect clinical outcomes of anatomic and reverse total shoulder arthroplasty.
The study is a non-randomized multi-center prospective registry and subjects will be treated according to standard of care at each center. Subjects will be approached for participation in this study after they have made the decision to undergo a primary or revision shoulder arthroplasty procedure. The treating surgeon will obtain verbal consent from the patient for a research coordinator to screen for eligibility. Patients who meet all criteria will be offered enrollment into the study. The total enrollment goal is a minimum of 500 anatomic shoulder arthroplasty and 500 reverse shoulder arthroplasty subjects enrolled in the multi-center registry.
Study Type
OBSERVATIONAL
Enrollment
2,500
Change in Pain
Measure of pain intensity. This is done with the Visual Analog Scare. (VAS)
Time frame: 10 years
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University of Arizona/Banner Health
Phoenix, Arizona, United States
RECRUITINGBanner Medical Group
Phoenix, Arizona, United States
RECRUITINGOrthopedic Surgery (Mayo Scottsdale)
Phoenix, Arizona, United States
RECRUITINGHCA Research Institute LLC.
Denver, Colorado, United States
RECRUITINGUniversity of Connecticut Health Center
Farmington, Connecticut, United States
TERMINATEDUniversity of Florida
Gainesville, Florida, United States
RECRUITINGAndrews Research & Education Foundation
Gulf Breeze, Florida, United States
RECRUITINGAdvent Health Orlando
Orlando, Florida, United States
RECRUITINGNorthShore University Health System
Evanston, Illinois, United States
WITHDRAWNThe Trustees of Indiana University
Indianapolis, Indiana, United States
RECRUITING...and 17 more locations